A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346802



Internal ID22202106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66879990..66882043hg38UCSC Ensembl
chr9:40810798..40812851hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204462
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346802
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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